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자료유형
학술저널
저자정보
Xizhe Zhao (Capital Medical University) Yi Li (Beijing Electric Power Hospital) Yan Yan (Beijing Electric Power Hospital) Xuelian Ma (Beijing Electric Power Hospital) Caixia Guo (Capital Medical University)
저널정보
한국유전학회 Genes & Genomics Genes & Genomics Vol.42 No.6
발행연도
2020.1
수록면
681 - 689 (9page)

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Background ACS (acute coronary syndrome), a subgroup of coronary artery disease (CHD), is a leading cause of death worldwide. Reports shown the association between methylation and CHD, while the abnormal expression of C1QTNF1 (C1q and tumor necrosis factor related protein 1) in CHD patients, but the underlying mechanisms are still unclear. Objective To analyze the methylation of CpG sites of C1QTNF1 in ACS patients. Methods Peripheral blood samples were collected from healthy controls and ACS patients. The methylation of total C1QTNF1, promoter sequence and CpG sites of C1QTNF1 were measured using methylation detection kits. The outcomes were compared between patients and controls based on gender, clinical classification and clinical stages. Results The promoter sequences from 37 ACS patients and 20 controls indicate that the methylation rate of C1QTNF1 was significantly lower in male patients compared to healthy controls at + 63 CpG sites (p = 0.03). Whereas, the methylation rate of C1QTNF1 in female patients was significantly lower than female health controls at − 89, + 39 and + 167 CpG sites (p = 0.021, 0.042, 0.021). In addition, the methylation rate of C1QTNF1 was significantly higher in male patients than female patients at − 89, − 41 and + 39 CpG sites (p = 0.011, 0.043, 0.006). Moreover, the methylation rate significantly decreased at − 24 sites (p = 0.021), but it significantly increased at − 14 site (p = 0.048) in patients with UA, compared to patients with STEMI (ST-segment elevation myocardial infarction). Conclusions There were significant differences in the methylation rate + 63 CpG sites between controls and male ACS patients. The − 14 site methylation increased in patients with UA, compared to patients with STEMI.

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